Permanganometry PDF
Permanganometry PDF
(permanganometry)
The concentration of a KMnO4 solution prepared from solid permanganate salt can not be
determined simply from tha weigh of the salt since the permanganate oxidizes the organic
impurities in the water, and the formed manganese dioxide catalyses the decomposition of KMnO 4
represented by the following equation:
Sodium oxalate or oxalic acid can be used to determine the exact concentration:
Additional indicator is not needed, the disappearance of the intense purple color of the
permanganate ions indicates the endpoint.
- ~0.63 g (COOH)2 2H2O is weighed on an analytical balance with the accuracy of 0.0001g and
100.0 cm3 of solution is prepared from it in a volumetric flask.
-10.0 cm3 of solution is transferred to 3 Erlenmeyer flasks with a pipette. The solutions are
acidified with ~5 cm3 of 20% sulfuric acid.
-The burette is rinsed with a few cm3 of the permanganate solution and the level is set to 0.0 .
-The oxalic acid solutions are warmed up to ~60 C. In the beginning the permanganate solution is
added very slowly (dropwise) since the reaction is catalyzed by the Mn(II) ions, later the reaction
becomes very fast. Titirating is continued until the last drop of KMnO 4 retains it's color and the
solution stays pink.
Titirate the given sample with the KMnO4 solution from the first exercise in the presence of
phosphoric acid (the phosphate complex of Fe(III) ions is colourless, so the yellow coloration of the
Fe(III) ions does not disturb the end point detection.